Have you heard of IPF? Are you affected by IPF?
Raremark IPF partnered with us at the Breathe Support Network to help our worldwide PF community become part of this virtual patchwork quilt for Global PF Awareness Month 2020. Click here to see more answers from patients and caregivers about how they #LIVEwithPF.
For #PFMonth, we asked real people to talk about how they #LIVEwithIPF!
The Breathe Support Network, established in June 2011, has become a premier online pulmonary fibrosis support network on the Facebook groups platform.
As a volunteer only organization, we enable patients and their loved ones to enjoy a better quality of life on the PF journey through peer to peer support, education and advocacy.
The Breathe Support Network (currently represented in 99 countries) is available worldwide for anyone on the PF journey, as well as those interested in learning more about pulmonary fibrosis.
Our peer-to-peer support is for PF patients and loved ones in all stages of the disease process.
The Breathe Support Network groups are FREE to everyone. A membership fee is not required to join. Our support groups are private. What you post in the groups stays within the groups. With 7 groups in our network, we have a group that is the right fit for you.
Because we are an online network, our doors are always open. 24 hours a day, 365 days a year, you can find support.
You may sign up for our mailing list in the box to the right. This list is for future communication in the event of a Facebook outage. Your private information will never be sold or distributed in any way.
Thank you from your Breathe Support Network team!
Breathe Support Network Groups